8 of 8 Statistical Programmer Jobs in Cambridge

Social network you want to login/join with: Senior Statistical Programmer, cambridge col-narrow-left Client: Warman O'Brien Location: Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 6 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Senior/Principal Statistical Programmers | Global CRO | UK | France | Poland | Spain | We are … partnering with a market-leading global CRO to recruit a Senior and/or Principal Statistical Programmer for a dynamic and high-impact role. This is not a traditional programming position, we’re looking for an experienced professional with robust, end-to-end programming expertise across multiple therapeutic areas. The ideal candidate will have a strong background in … Spain, or Poland. What to do next: If this opportunity is of interest, please apply now with your CV as the organisation are looking to welcome the Senior & Principal Statistical Programmers onboard as soon as possible. Not what you’re looking for? Please contact Jo Fornaciari on +44 7488 822 859 for a confidential discussion about potential opportunities. #J More ❯

Social network you want to login/join with: Principal Statistical Programmer, cambridge col-narrow-left Client: Warman O'Brien Location: Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 4 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Principal Statistical Programmer | Leading CRO | Home Based | UK | Join a fast-growing … organisation offers a flexible, dynamic, and entrepreneurial culture. With ongoing growth and exciting career opportunities, it’s the perfect place to advance your career. We’re seeking elite Principal Statistical Programmers to join this growing organisation remotely from anywhere in the UK. What you will be doing: You’ll lead statistical programming projects, ensuring high-quality, on-time … compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data structures e.g. CDISC, SDTM, ADaM, Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines. More ❯

Social network you want to login/join with: Senior Statistical Programmer - UK (Remote/Office/Hybrid), Cambridge Client: Veramed Location: UK Job Category: Other EU work permit required: Yes Job Views: 4 Posted: 06.06.2025 Expiry Date: 21.07.2025 Job Description: Veramed prides itself on providing high-quality statistics and programming consultancy, along with an industry-leading working … environment supporting career growth. We are seeking Senior Statistical Programmers in the UK for a permanent position. We offer flexible working arrangements, training, support, and a competitive package. The role involves providing programming support across various projects, clients, and therapeutic areas. Key Responsibilities Technical Perform consistency review of clinical trial documents (protocols, SAPs, CRFs, CSRs) Author and review study … standards Conduct data checks and exploration (e.g., frequencies, histograms) Program and QC datasets and TFLs in SAS following specifications Review CDISC Validation reports Ensure standards compliance Familiarity with basic statistical techniques (t-test, ANOVA, regression, survival analysis) Review project management documents Maintain audit-ready study documents General Lead study team meetings Present study updates Share knowledge within the team More ❯

Job Title: Senior Statistical Programmer I Career Level - D Introduction to role The Senior Statistical Programmer I is a delivery-focused role responsible for programming deliverables with quality and timeliness, following established standards and processes. This position requires technical skills and adequate industry knowledge to independently perform programming tasks while using judgment about seeking guidance in … will drive continuous improvement. Accountabilities Collaborate with other team members to provide programming support to deliver technical programming and information components of a study or a project deliverable Implement statistical programming aspects of the protocol or clinical development program Ensure high quality is built into own deliverables and the deliverables of other programmers on the team Program independently with … activities and tasks Identify and communicate risk within the assigned studies and/or projects Work cooperatively with study team members including but not limited to the statistician, lead programmer, data manager, and study leader Work cooperatively with contract programming providers Contribute to technical initiatives Employ basic project management practices in managing programming aspects of drug or technical projects More ❯

This role is considered Hybrid. Principal Statistical Programmer The Principal Statistical Programmer will provide expert-level hands-on principal programming support and technical leadership to develop, maintain, validate and run SAS computer programs that access, visualize, analyze, and report clinical trial data, in accordance with statistical analysis plans, ICH guidelines, and applicable regulatory requirements. The … SAS code; Write specifications to describe programming needs; Create and validate global macros or systems that streamline repetitive operations to increase programming efficiency; Keep abreast of current and new statistical programming techniques and other applicable technical advancements while assisting in their implementation; Provide input into, or lead general standardization efforts (e.g., CRFs, query checks, standard statistical programs, data … presentations); Assist or lead efforts to develop programming processes consistent with industry best practices; Review DMP, eCRF specs, and other clinical data management documents; Review statistical analysis plans and other related documents; Partner with or oversee CROs or Programming vendors to perform any of the above tasks; Other duties as assigned. Qualifications At least 8 years' industry (Pharmaceutical, Biotech More ❯

week ago Be among the first 25 applicants Job Title: Senior Statistical Programmer II Career Level: D Introduction to role: Are you ready to take on a pivotal role in the development and validation of programs that create datasets conforming to Alexion and CDISC standards? As a Senior Statistical Programmer II, you will be at the … complexity, you may lead programming efforts, ensuring alignment with ICH guidelines, Good Clinical Practices, and regulatory requirements. You'll also have the opportunity to mentor fellow programmers and represent Statistical Programming in meetings with internal and external clients. Are you prepared to integrate statistical concepts with SAS Programming efficiently and effectively? Accountabilities: Support development of technical programming specifications … ideas and thoughts towards the optimization of standard operating procedures. Lead team meetings when appropriate. Any other activities as required. Essential Skills/Experience: Minimum of 6 years of statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry. Proven ability to: Develop and validate technical specifications and programs for safety and efficacy analysis datasets, tables, listings, and More ❯

days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Job Title: Principal Statistical Programmer Introduction to role: Are you ready to make a significant impact in the world of biopharmaceuticals? As a Principal Statistical Programmer, you'll be at the forefront of developing and validating programs … data through Tables, Listings, and Figures (TLFs). You'll ensure compliance with ICH guidelines, Good Clinical Practices, and regulatory requirements while leading programming efforts and representing Clinical and Statistical Programming in meetings with internal and external clients. As a mentor to other Statistical Programmers, you'll integrate statistical concepts with SAS Programming efficiently and optimally. Accountabilities … required. Essential Skills/Experience: Bachelor’s Degree (Minimum) or Master’s Degree or equivalent experience (Preferred) in Biostatistics, Statistics or another related field Minimum of 7 years of statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry. Proven ability to: Develop and validate technical specifications and programs for safety and efficacy analysis datasets, tables, listings, and More ❯

Social network you want to login/join with: Senior Statistical Programmer I, cambridge col-narrow-left Client: Warman O'Brien Location: Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 2 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: Senior Statistical Programmer I - Join a World-Leading CRO! Join a … globally renowned CRO that is expanding its Statistical Programming team across the UK and Europe. This innovative organisation is driven by excellence and firmly believes in investing in its people, recognizing them as its greatest strength and the driving force behind its success. As a Senior Statistical Programmer I, you will lead studies of varying complexity, working … planned technology expansion journey, gaining exposure to other languages such as R or Python. What you’ll be doing: Lead Phase II/III studies, crafting, validating, and executing statistical programs for listings, safety, efficacy outputs, and ADaM/TLF specifications. Oversee multi-disciplinary teams, ensuring seamless execution of assigned projects. Design, develop, validate, and execute high-quality SAS More ❯